Veeva Clinical Software Engineer II

By Admin · IT & Software in Life Sciences

HYDERABAD (IN)ONSITEPOSTED: 9/9/2026
TECHFull-time
HIRING ORGANIZATIONBRISTOL MYERS SQUIBBPharmaceuticals
BR

ROLE OVERVIEW

Lead delivery and operations of Veeva Clinical and Platform capabilities while mentoring developers, partnering with business stakeholders, and ensuring secure, reliable, compliant technology solutions.

ROLE DEFINITION & RESPONSIBILITIES

  • •Own end-to-end reliability, accessibility, security, and compliance of Veeva technology assets
  • •Mentor Veeva developers across Quality, Regulatory, Clinical, and Platform domains
  • •Lead maintenance, break-fix releases, security assessments, regulatory risk assessments, and incident response
  • •Manage Veeva Vault build-and-run activities and coordinate General, Operational, and Project Releases
  • •Collaborate with Veeva Cloud teams to understand domain-specific Vault capabilities
  • •Partner with IT Business Partners and business SMEs to prioritize, deliver, and support technology solutions
  • •Design technical solutions aligned with business requirements and communicate IT needs to stakeholders
  • •Maintain technology-specific business capabilities and pursue Veeva Associate Administrator certification
Reporting Hierarchy: Reports to the Veeva Platform community lead in the India center; leads a small team and works in a matrix structure with Veeva developers, testers, internal teams, contractors, and Veeva product teams.

* Role responsibilities and qualifications synthesized based on industry benchmark standards.

QUALIFICATIONS & REQUIREMENTS

REQUIRED QUALIFICATIONS

  • University degree with 5-7 years of relevant experience
  • 5+ years of validated-system Computer System Validation experience
  • 3+ years of Quality, Regulatory, Clinical, and Platform Vault experience
  • Knowledge of GMP, Quality, Regulatory, Clinical Management System, and related Docs capabilities
  • People-management and matrix-team leadership experience
  • Strong stakeholder communication, negotiation, analytical thinking, and coaching capabilities

PREFERRED QUALIFICATIONS

  • •Veeva White Belt certification
  • •Experience with Veeva Associate Administrator certification or administration
  • •Broader Veeva Vault implementation and operations experience
  • •Experience leading process improvement and moderately complex technology solutions

REQUIRED VERIFIED SKILLS

Veeva Vault
Veeva Clinical
Veeva Quality
Veeva Regulatory
Veeva Platform
Computer System Validation
GMP
clinical systems
regulatory systems
quality systems
technology asset management
incident response
security risk assessment
release management

COMPENSATION & REWARDS

Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Comprehensive benefits, wellbeing support, flexible work options, professional development, inclusive workplace, and employee support programs, subject to applicable local terms
No salary range is disclosed in the supplied posting. Compensation should be evaluated based on the candidate's Veeva expertise, regulated-systems experience, leadership scope, and the Hyderabad life-sciences technology market.

ORGANIZATION CONTEXT & CULTURE

Bristol Myers Squibb is a purpose-driven biopharmaceutical company focused on discovering, developing, and delivering innovative medicines for serious diseases.

TEAM SIZE: 30,000+ employees
INDUSTRY: Pharmaceuticals
Culture: Purpose-driven, collaborative, accountable, inclusive, innovative, and focused on patient impact, employee wellbeing, flexibility, and continuous growth.

EXPECTED CAREER ROADMAP

Offers progression toward Veeva platform leadership, clinical technology management, enterprise application architecture, technology product ownership, or broader life-sciences IT leadership roles. Strong performance can also expand responsibility across regulated technology portfolios and people management.

APPLICATION ADVISORY

Emphasize Veeva Vault and Clinical/Quality/Regulatory/Platform experience; clearly quantify validated-system CSV experience; highlight GMP and regulated-environment knowledge; demonstrate release, incident, security, and compliance ownership; showcase people leadership and matrix collaboration; mention Veeva certifications prominently; provide examples of stakeholder negotiation and measurable process improvements.

READY TO SUBMIT?

Verify your capability profile and matching credentials before submitting direct applications.